Hansen C - Search Results

1

Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect.

Schulze A, Hansen C, Baekgaard P, Blichfeldt S, Petersen MB, Tommerup N, Brøndum-Nielsen K. Schulze A, et al. Among authors: hansen c. Acta Paediatr. 1997 Aug;86(8):906-10. doi: 10.1111/j.1651-2227.1997.tb08622.x. Acta Paediatr. 1997. PMID: 9307178

2

Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.

Schulze A, Hansen C, Skakkebaek NE, Brøndum-Nielsen K, Ledbeter DH, Tommerup N. Schulze A, et al. Among authors: hansen c. Nat Genet. 1996 Apr;12(4):452-4. doi: 10.1038/ng0496-452. Nat Genet. 1996. PMID: 8630505

3

MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern.

Nielsen JB, Henriksen KF, Hansen C, Silahtaroglu A, Schwartz M, Tommerup N. Nielsen JB, et al. Among authors: hansen c. Eur J Hum Genet. 2001 Mar;9(3):178-84. doi: 10.1038/sj.ejhg.5200600. Eur J Hum Genet. 2001. PMID: 11313756

4

Assignment of the human zinc finger gene, ZNF288, to chromosome 3 band q13.2 by radiation hybrid mapping and fluorescence in situ hybridisation.

Harboe TL, Tümer Z, Hansen C, Jensen NA, Tommerup N. Harboe TL, et al. Among authors: hansen c. Cytogenet Cell Genet. 2000;89(3-4):156-7. doi: 10.1159/000015600. Cytogenet Cell Genet. 2000. PMID: 10965110 No abstract available.

5

Human rab11a: transcription, chromosome mapping and effect on the expression levels of host GTP-binding proteins.

Gromov PS, Celis JE, Hansen C, Tommerup N, Gromova I, Madsen P. Gromov PS, et al. Among authors: hansen c. FEBS Lett. 1998 Jun 16;429(3):359-64. doi: 10.1016/s0014-5793(98)00607-3. FEBS Lett. 1998. PMID: 9662449 Free article.

6

Isolation of the human beaded-filament structural protein 1 gene (BFSP1) and assignment to chromosome 20p11.23-p12.1.

Rendtorff ND, Hansen C, Silahtaroglu A, Henriksen KF, Tommerup N. Rendtorff ND, et al. Among authors: hansen c. Genomics. 1998 Oct 1;53(1):114-6. doi: 10.1006/geno.1998.5478. Genomics. 1998. PMID: 9787085 No abstract available.

7

The human hedgehog-interacting protein gene: structure and chromosome mapping to 4q31.21-->q31.3.

Bak M, Hansen C, Friis Henriksen K, Tommerup N. Bak M, et al. Among authors: hansen c. Cytogenet Cell Genet. 2001;92(3-4):300-3. doi: 10.1159/000056918. Cytogenet Cell Genet. 2001. PMID: 11435703

8

Cloning, characterization and chromosomal localization of the Sus scrofa SLC31A1 gene.

Harboe TL, Jensen LR, Hansen C, Horn P, Bendixen C, Tommerup N, Tümer Z. Harboe TL, et al. Among authors: hansen c. Anim Genet. 2003 Feb;34(1):59-61. doi: 10.1046/j.1365-2052.2003.00940.x. Anim Genet. 2003. PMID: 12580789

9

Sequence variants in the human cocaine and amphetamine-regulated transcript (CART) gene in subjects with early onset obesity.

Echwald SM, Sørensen TI, Andersen T, Hansen C, Tommerup N, Pedersen O. Echwald SM, et al. Among authors: hansen c. Obes Res. 1999 Nov;7(6):532-6. doi: 10.1002/j.1550-8528.1999.tb00710.x. Obes Res. 1999. PMID: 10574510 Free article.

10

Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.

Møller RS, Kübart S, Hoeltzenbein M, Heye B, Vogel I, Hansen CP, Menzel C, Ullmann R, Tommerup N, Ropers HH, Tümer Z, Kalscheuer VM. Møller RS, et al. Among authors: hansen cp. Am J Hum Genet. 2008 May;82(5):1165-70. doi: 10.1016/j.ajhg.2008.03.001. Epub 2008 Apr 10. Am J Hum Genet. 2008. PMID: 18405873 Free PMC article.

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